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Healthy Individuals clinical trials

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NCT ID: NCT06137534 Completed - Healthy Individuals Clinical Trials

Upper Extremity Pattern Exercises and Respiratory Functions

Start date: November 10, 2023
Phase: N/A
Study type: Interventional

The study will be carried out with healthy students between the ages of 18-25 years who are studying at Ege University Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation and who voluntarily agree to participate in the study. Informed consent form will be signed before the evaluation of the individuals. The study will be carried out as a single group with the inclusion of a total of 20 individuals. The students who volunteered to participate in the study will actively apply the selected PNF upper extremity patterns for 4 weeks and will be evaluated twice, before and after the application. Demographic information of the individuals; age, height, weight, gender, background, surname, smoking habit, alcohol habit, education level (class), sports habit, COVID-19 disease status and when it occurred will be recorded. Cosmed pulmonary function test device will be used to evaluate the respiratory function of the individuals, Oncomed brand electronic body weight and height measurement device will be used to calculate the body mass index. Body Image Perception Scale will be used for body image perception, Beck Depression Inventory will be used to evaluate psychological status, and Rosenberg Self-Esteem Scale will be used to evaluate sense of self.

NCT ID: NCT06044896 Completed - Healthy Individuals Clinical Trials

Physiology of Body Lateralization on Regional Lung Ventilation Study

LATLUNGS
Start date: September 22, 2023
Phase: N/A
Study type: Interventional

The goal of this experimental study, with crossover design, is to analyze the effects of body lateralization applied at 30 degrees compared to the supine position on the distribution of ventilation and regional lung aeration in healthy individuals. The main study questions to be answered are: - Question 1: What are the immediate effects of 30 degree body lateralization on the distribution of regional ventilation and lung aeration in healthy individuals? - Question 2: What is the effect of body lateralization on diaphragmatic mobility in the dependent or non-dependent hemithorax? Participants will be submitted to changes in positioning in bed, considering a randomized sequence of interventions, between supine position and body lateralization at 30 degrees, using the Multicare bed (Linet, Czech Republic). The interventions were repeated twice each with a 30-minute washout in each sequence. Participants will perform assessment of lung function and respiratory muscle strength with the instruments: - Manovacuometry - Spirometry - Ventilometry - Respiratory Diagnostic Assistant The supine and body lateralization positions will be compared, with the primary outcomes being lung aeration and ventilation distribution assessed using Electrical Impedance Tomography. The secondary outcome will be diaphragmatic mobility measured through lung ultrasound. Groups: - Supine position - Body lateralization Effects - Lung aeration - Distribution of ventilation - Diaphragmatic mobility

NCT ID: NCT05637060 Completed - Healthy Individuals Clinical Trials

Bioequivalence Study of Rosuvastatin Tablet

BE
Start date: November 24, 2022
Phase: N/A
Study type: Interventional

This study is designed to explore the bioequivalence of Test Product Vaptor (Rosuvastatin) 20 mg Tablet with the reference product Crestor (Rosuvastatin) 20 mg tablet under fasting conditions in healthy Pakistani male subjects.

NCT ID: NCT05597657 Completed - Healthy Individuals Clinical Trials

Normal Variation of T1 Values With Cardiac Magnetic Resonance in Healthy Individuals

NATIVE
Start date: October 12, 2021
Phase: N/A
Study type: Interventional

The purpose of the study is to determine the normal variation of T1 values with cardiac magnetic resonance in healthy individuals with respect to reproducibility, changes over time, and dependency on hydration status.

NCT ID: NCT05541094 Completed - Healthy Individuals Clinical Trials

Study of Vitamin D Fortification of Milk and Oil

Tata
Start date: October 13, 2020
Phase:
Study type: Observational

It is a two-year longitudinal effectiveness study. A comparative study with a case-control design. Study will be conducted in Pune city. A total of up to 100 families (50 families per group) will be recruited. The test group will consist of families consuming fortified milk and oil and the control group will consist of families consuming non fortified milk and oil. Individuals between the age 5-18 years, 18-50 years and more than 50 years will be enrolled. Families which intend to stay in the city for the next 2 years, willing to continue with the same brand of milk and oil for the next 2 years, children living with their biological parents and families willing to sign consent form, will be enrolled in the study. Individuals having chronic illnesses likely to affect vitamin D concentrations and those allergic to milk will be excluded.

NCT ID: NCT05011968 Completed - Healthy Individuals Clinical Trials

Intervention Study on Iodine Biofortification Vegetables ( Nutri-I-Food

Nutri-I-Food
Start date: March 1, 2019
Phase: N/A
Study type: Interventional

The aim of the project is to study of the influence of Lettuce crop enriched with Iodine on Thyroid hormone synthesis. Secondary outcome to find out iodine presence in urine in order to evaluate vegetables, like little crop, as Iodine biocarrier

NCT ID: NCT04941196 Completed - Healthy Individuals Clinical Trials

Bioequivalence Study of Anplag® 90mg (Ticagrelor) Tablet & Brilinta® 90 mg (Ticagrelor) Tablet in Healthy Adult Male Pakistani Subjects Under Fasting Condition

BE
Start date: October 16, 2020
Phase: Phase 1
Study type: Interventional

Single oral administration of study drugs (i.e. Anplag® & Brilinta®) in Two periods after at least 10 hours fasting. The periods will be separated by a washout period of 7 days. The purpose of this study is to compare the bioavailability of Anplag® 90mg (Ticagrelor) Tablet with Brilinta® 90 mg (Ticagrelor) Tablet under fasting conditions in healthy Pakistani male subjects.

NCT ID: NCT04873570 Completed - Healthy Individuals Clinical Trials

Bioequivalence Study of Mofest® 400mg (Moxifloxacin) Tablet With Avelox® 400mg (Moxifloxacin) Tablet in Healthy Pakistani Subjects

BE
Start date: May 28, 2021
Phase: Phase 1
Study type: Interventional

Single oral dose, of test and reference Tablet will be administered to healthy volunteers, after at least 10 hours fast together with 240 mL of ambient temperature water at their scheduled dosing time-points. Blood samples will be taken up to 72.0 hours post-dose.

NCT ID: NCT04830098 Completed - Healthy Individuals Clinical Trials

Comparison of the Effectiveness of Spinal Stabilization Exercises and Chiropractic Spinal Manipulation

Start date: March 5, 2021
Phase: N/A
Study type: Interventional

It is the study of the effectiveness of spinal stabilization exercises and chiropractic spinal manipulation in healthy individuals. In addition, it was planned to investigate the effects of spinal stabilization exercises and manipulation on muscle strength, muscular endurance, balance and proprioception, depression and quality of life.

NCT ID: NCT04772417 Completed - Healthy Individuals Clinical Trials

The Effects of Standardized vs Individualized Seat Height on 1-minute Sit-to-stand Performance

ESTI-STS
Start date: April 20, 2021
Phase:
Study type: Observational

The 1-minute sit-to-stand test (1MSTS) is a widely used functional capacity test and has promising predictive potential. Current standards of practice suggest the use of a chair with a standardized height. However, this practice makes the test more demanding for taller individuals than for shorter individuals. This implies over- or underestimation of functional capacity depending on body morphology. Therefore, the aim of this study is to investigate the influence of knee joint angle, femur length and bodyweight on the 1MSTS performance in healthy subjects with different morphology.